U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 163

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146846insertion1nstd232human GRCh37.p13 chr17: 40,968,072-40,968,072 , GRCh38.p12 chr17: 42,816,054-42,816,054 BECN1
    nsv6991508copy number variation1nstd229human GRCh38 chr17: 42,821,629-43,873,068 , GRCh37.p13 chr17: 40,973,647-41,950,436 RND2, LOC107985077, 50 more genes
    nsv6985364copy number variation1nstd229human GRCh38 chr17: 42,723,977-42,924,183 , GRCh37.p13 chr17: 40,875,995-41,076,200 AOC2, WNK4, 15 more genes
    nsv6985178copy number variation1nstd229human GRCh38 chr17: 42,812,572-42,819,644 , GRCh37.p13 chr17: 40,964,590-40,971,662 BECN1
    nsv6984984copy number variation1nstd229human GRCh38 chr17: 38,377,708-42,855,253 , GRCh37.p13 chr17: 36,701,616-41,007,270 ZNF385C, AOC2, 248 more genes
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6982041copy number variation1nstd229human GRCh38 chr17: 42,816,137-42,820,313 , GRCh37.p13 chr17: 40,968,155-40,972,331 BECN1
    nsv6592373inversion1nstd223human GRCh38 chr17: 42,812,612-42,813,131 , GRCh37.p13 chr17: 40,964,630-40,965,149 BECN1
    nsv6583749inversion1nstd223human GRCh38 chr17: 42,812,724-42,812,988 , GRCh37.p13 chr17: 40,964,742-40,965,006 BECN1
    nsv6511710copy number variation1nstd223human GRCh38 chr17: 42,823,399-42,826,552 , GRCh37.p13 chr17: 40,975,417-40,978,569 MIR6781, BECN1
    nsv6510942copy number variation1nstd223human GRCh38 chr17: 42,810,927-42,811,653 , GRCh37.p13 chr17: 40,962,945-40,963,671 BECN1, CNTD1
    nsv6133246copy number variation1nstd213human GRCh37 chr17: 40,670,000-41,570,001 , GRCh38.p12 chr17: 42,517,982-43,492,633 AOC2, ARL4D, 65 more genes
    nsv6034583copy number variation1nstd212human GRCh38 chr17: 42,813,066-42,813,126 , GRCh37.p13 chr17: 40,965,084-40,965,144 BECN1
    nsv6021553copy number variation1nstd212human GRCh38 chr17: 42,812,115-42,812,292 , GRCh37.p13 chr17: 40,964,133-40,964,310 BECN1
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5537057insertion1nstd206human GRCh38 chr17: 42,816,857-42,816,859 , GRCh37.p13 chr17: 40,968,875-40,968,877 BECN1
    nsv5157533mobile element insertion1nstd203human GRCh38 chr17: 42,816,808-42,816,857 , GRCh37.p13 chr17: 40,968,826-40,968,875 BECN1
    nsv5143936mobile element insertion1nstd203human GRCh38 chr17: 42,812,361-42,812,384 , GRCh37.p13 chr17: 40,964,379-40,964,402 BECN1
    nsv4743380copy number variation1nstd199human GRCh37 chr17: 40,965,083-40,965,139 , GRCh38.p12 chr17: 42,813,065-42,813,121 BECN1
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center